Mutagenetix > Incidental Mutation

Incidental Mutation 'R9198:Dnah9'

698062

Institutional Source

Beutler Lab

Gene Symbol

Dnah9

Ensembl Gene

ENSMUSG00000056752

Gene Name

dynein, axonemal, heavy chain 9

Synonyms

D11Ertd686e, Dnahc9

MMRRC Submission

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.400) question?

Stock #

R9198 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

65722150-66059379 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 65846570 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 2914 (N2914S)

Ref Sequence

ENSEMBL: ENSMUSP00000079494 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080665]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000080665
AA Change: N2914S

PolyPhen 2 Score 0.018 (Sensitivity: 0.95; Specificity: 0.80)

SMART Domains

Protein: ENSMUSP00000079494
Gene: ENSMUSG00000056752
AA Change: N2914S

Domain	Start	End	E-Value	Type
Pfam:DHC_N1	209	787	3.6e-164	PFAM
coiled coil region	788	820	N/A	INTRINSIC
low complexity region	1228	1240	N/A	INTRINSIC
Pfam:DHC_N2	1290	1699	1.4e-134	PFAM
AAA	1863	1999	4.9e-1	SMART
AAA	2141	2341	1.99e0	SMART
AAA	2468	2614	6.75e-1	SMART
Pfam:AAA_8	2786	3053	1.1e-165	PFAM
Pfam:MT	3065	3408	7.2e-208	PFAM
Pfam:AAA_9	3430	3652	3.2e-87	PFAM
Pfam:Dynein_heavy	3786	4482	1e-241	PFAM

Predicted Effect

SMART Domains

Protein: ENSMUSP00000116499
Gene: ENSMUSG00000056752
AA Change: N463S

Domain	Start	End	E-Value	Type
Pfam:AAA_7	1	258	3e-155	PFAM
Pfam:AAA_8	336	603	3.9e-166	PFAM
Pfam:MT	615	958	2.3e-208	PFAM
Pfam:AAA_9	980	1202	1.1e-87	PFAM
Pfam:Dynein_heavy	1336	1514	2.4e-52	PFAM
Pfam:Dynein_heavy	1508	1956	8.6e-155	PFAM

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.9%
20x: 99.5%

Validation Efficiency

97% (61/63)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the heavy chain subunit of axonemal dynein, a large multi-subunit molecular motor. Axonemal dynein attaches to microtubules and hydrolyzes ATP to mediate the movement of cilia and flagella. The gene expresses at least two transcript variants; additional variants have been described, but their full length nature has not been determined. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam22	A	G	5: 8,167,583 (GRCm39)		probably null	Het
Adamts9	A	T	6: 92,837,170 (GRCm39)	S1164T	probably benign	Het
Bcat1	A	T	6: 144,985,222 (GRCm39)	I140N	probably damaging	Het
Bod1l	T	C	5: 41,957,129 (GRCm39)	T2832A	probably benign	Het
Brca2	A	T	5: 150,459,977 (GRCm39)	E417D	possibly damaging	Het
Ccdc88b	T	C	19: 6,831,268 (GRCm39)	D558G	possibly damaging	Het
Ccdc88b	T	C	19: 6,833,213 (GRCm39)	E278G	probably damaging	Het
Celsr1	G	T	15: 85,917,286 (GRCm39)	S229*	probably null	Het
Cenpf	G	T	1: 189,388,987 (GRCm39)	T1615K	probably damaging	Het
Cep250	T	C	2: 155,830,354 (GRCm39)		probably null	Het
Clec4d	T	C	6: 123,251,757 (GRCm39)	F213S	probably damaging	Het
Clip4	G	A	17: 72,117,884 (GRCm39)	G310R	probably damaging	Het
Csmd1	G	A	8: 15,962,430 (GRCm39)	R3255W	probably damaging	Het
Ctsm	T	C	13: 61,687,612 (GRCm39)	D82G	probably damaging	Het
Cyp26a1	A	G	19: 37,686,790 (GRCm39)	T81A	probably damaging	Het
Dld	A	G	12: 31,390,885 (GRCm39)	V187A	probably benign	Het
Dmrt2	T	A	19: 25,655,477 (GRCm39)	Y359N	probably benign	Het
Dpyd	A	T	3: 118,553,303 (GRCm39)		probably null	Het
Fgl2	A	C	5: 21,577,920 (GRCm39)	Q69P	probably damaging	Het
Gadd45gip1	A	T	8: 85,560,780 (GRCm39)	I132F	probably damaging	Het
Gm15446	T	C	5: 110,090,743 (GRCm39)	C332R	probably damaging	Het
Gm15737	A	T	6: 92,856,640 (GRCm39)	E23V	unknown	Het
Gm5111	A	G	6: 48,567,037 (GRCm39)	H84R	unknown	Het
Golga3	G	A	5: 110,355,619 (GRCm39)	S991N	probably benign	Het
H2-M10.3	A	G	17: 36,678,919 (GRCm39)	Y50H	probably damaging	Het
Hivep2	C	T	10: 14,005,621 (GRCm39)	H740Y	probably benign	Het
Il18rap	C	T	1: 40,582,177 (GRCm39)	T366M	probably benign	Het
Ints7	T	A	1: 191,351,872 (GRCm39)	S860R	probably benign	Het
Lipi	T	A	16: 75,362,461 (GRCm39)	T217S	possibly damaging	Het
Lrrc2	G	T	9: 110,791,722 (GRCm39)	C158F	probably benign	Het
Lrrc30	T	C	17: 67,938,854 (GRCm39)	D242G	probably benign	Het
Map1a	A	T	2: 121,133,854 (GRCm39)	M1557L	probably benign	Het
Matn2	A	G	15: 34,423,924 (GRCm39)	E594G	probably damaging	Het
Mfsd12	T	C	10: 81,198,544 (GRCm39)	L345P	probably damaging	Het
Mmp24	A	G	2: 155,640,041 (GRCm39)	R124G	probably benign	Het
Ngef	T	A	1: 87,406,797 (GRCm39)	H240L	unknown	Het
Nmur1	T	G	1: 86,315,256 (GRCm39)	D203A	probably benign	Het
Nt5c3	T	C	6: 56,859,955 (GRCm39)	Q328R	probably benign	Het
Ogfr	T	C	2: 180,232,850 (GRCm39)		probably null	Het
Or4k1	A	T	14: 50,377,990 (GRCm39)	Y35*	probably null	Het
Or52ac1	T	A	7: 104,245,635 (GRCm39)	Y251F	probably damaging	Het
Or5h19	A	G	16: 58,856,263 (GRCm39)	V279A	probably benign	Het
Osbpl10	G	A	9: 115,061,211 (GRCm39)	W588*	probably null	Het
Pask	A	T	1: 93,265,205 (GRCm39)	S17T	possibly damaging	Het
Pfkfb3	C	T	2: 11,491,084 (GRCm39)	R170K	probably damaging	Het
Plec	A	G	15: 76,069,937 (GRCm39)	C960R	unknown	Het
Pramel11	T	A	4: 143,623,646 (GRCm39)	N176I	probably benign	Het
R3hdm2	T	G	10: 127,293,521 (GRCm39)	S142A	probably damaging	Het
Rfx7	T	C	9: 72,524,163 (GRCm39)	L451P	probably damaging	Het
Rimbp2	T	A	5: 128,883,552 (GRCm39)	E76V	probably damaging	Het
Rock2	A	G	12: 17,015,557 (GRCm39)	N818S	probably benign	Het
Ryk	A	T	9: 102,758,854 (GRCm39)	I248F	possibly damaging	Het
Setd2	A	G	9: 110,378,168 (GRCm39)	Q661R	possibly damaging	Het
Siae	T	C	9: 37,539,105 (GRCm39)	V172A	probably benign	Het
Slc35f4	A	G	14: 49,556,377 (GRCm39)	S9P	unknown	Het
Smg1	T	C	7: 117,795,179 (GRCm39)	E456G	unknown	Het
Srgap3	C	T	6: 112,743,865 (GRCm39)	A458T	probably damaging	Het
Tgfbrap1	T	A	1: 43,093,799 (GRCm39)	R564S	probably damaging	Het
Usp15	A	G	10: 123,004,143 (GRCm39)	Y204H	probably damaging	Het
Usp35	A	G	7: 96,962,276 (GRCm39)	Y527H	probably damaging	Het
Usp8	T	A	2: 126,600,524 (GRCm39)	*1092K	probably null	Het
Vmn2r73	A	T	7: 85,518,987 (GRCm39)	M545K	probably benign	Het
Ylpm1	A	T	12: 85,080,689 (GRCm39)		probably null	Het
Zscan22	G	T	7: 12,641,130 (GRCm39)	R458L	probably damaging	Het

Other mutations in Dnah9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00696:Dnah9	APN	11	65,732,064 (GRCm39)	splice site	probably benign
IGL00805:Dnah9	APN	11	65,772,521 (GRCm39)	missense	probably benign	0.00
IGL00826:Dnah9	APN	11	65,880,768 (GRCm39)	missense	probably damaging	1.00
IGL01108:Dnah9	APN	11	65,740,806 (GRCm39)	missense	possibly damaging	0.93
IGL01152:Dnah9	APN	11	65,962,882 (GRCm39)	missense	probably damaging	1.00
IGL01353:Dnah9	APN	11	65,971,397 (GRCm39)	missense	probably damaging	1.00
IGL01364:Dnah9	APN	11	66,046,285 (GRCm39)	missense	probably damaging	1.00
IGL01479:Dnah9	APN	11	65,846,543 (GRCm39)	missense	probably benign	0.14
IGL01537:Dnah9	APN	11	65,838,506 (GRCm39)	missense	probably benign
IGL01565:Dnah9	APN	11	65,924,655 (GRCm39)	missense	possibly damaging	0.95
IGL01597:Dnah9	APN	11	66,009,656 (GRCm39)	missense	probably damaging	1.00
IGL01619:Dnah9	APN	11	65,722,441 (GRCm39)	nonsense	probably null
IGL01625:Dnah9	APN	11	65,935,471 (GRCm39)	missense	probably damaging	1.00
IGL01803:Dnah9	APN	11	66,009,655 (GRCm39)	missense	probably damaging	1.00
IGL01819:Dnah9	APN	11	65,998,952 (GRCm39)	missense	probably benign	0.33
IGL01896:Dnah9	APN	11	66,021,492 (GRCm39)	missense	possibly damaging	0.89
IGL01922:Dnah9	APN	11	65,965,860 (GRCm39)	splice site	probably benign
IGL01923:Dnah9	APN	11	66,016,061 (GRCm39)	splice site	probably benign
IGL02059:Dnah9	APN	11	65,963,784 (GRCm39)	missense	probably damaging	1.00
IGL02068:Dnah9	APN	11	65,951,871 (GRCm39)	missense	probably damaging	1.00
IGL02135:Dnah9	APN	11	66,008,318 (GRCm39)	missense	possibly damaging	0.63
IGL02146:Dnah9	APN	11	65,818,526 (GRCm39)	missense	probably damaging	1.00
IGL02264:Dnah9	APN	11	65,971,314 (GRCm39)	splice site	probably benign
IGL02325:Dnah9	APN	11	65,725,043 (GRCm39)	missense	probably damaging	1.00
IGL02426:Dnah9	APN	11	66,015,979 (GRCm39)	missense	probably benign
IGL02440:Dnah9	APN	11	65,846,072 (GRCm39)	missense	probably damaging	1.00
IGL02471:Dnah9	APN	11	65,838,444 (GRCm39)	nonsense	probably null
IGL02496:Dnah9	APN	11	65,920,189 (GRCm39)	missense	probably damaging	1.00
IGL02672:Dnah9	APN	11	65,818,427 (GRCm39)	missense	probably benign	0.02
IGL02718:Dnah9	APN	11	65,777,466 (GRCm39)	missense	probably damaging	0.99
IGL02832:Dnah9	APN	11	65,931,172 (GRCm39)	missense	probably damaging	1.00
IGL02851:Dnah9	APN	11	65,928,570 (GRCm39)	splice site	probably benign
IGL02859:Dnah9	APN	11	65,772,445 (GRCm39)	splice site	probably benign
IGL02864:Dnah9	APN	11	65,951,829 (GRCm39)	missense	probably damaging	1.00
IGL02954:Dnah9	APN	11	66,009,793 (GRCm39)	missense	probably damaging	1.00
IGL02987:Dnah9	APN	11	65,732,099 (GRCm39)	missense	probably benign	0.23
IGL02987:Dnah9	APN	11	65,746,098 (GRCm39)	missense	probably damaging	0.98
IGL03160:Dnah9	APN	11	65,998,880 (GRCm39)	missense	probably damaging	0.98
IGL03171:Dnah9	APN	11	65,872,067 (GRCm39)	missense	probably benign	0.13
IGL03180:Dnah9	APN	11	65,777,465 (GRCm39)	missense	probably damaging	0.99
IGL03388:Dnah9	APN	11	65,838,368 (GRCm39)	missense	probably damaging	1.00
anarchy	UTSW	11	65,846,074 (GRCm39)	missense	probably damaging	0.99
sacco	UTSW	11	66,058,905 (GRCm39)	missense	possibly damaging	0.82
Tweed	UTSW	11	65,962,898 (GRCm39)	missense	probably damaging	0.99
vanzetti	UTSW	11	65,746,198 (GRCm39)	nonsense	probably null
IGL02837:Dnah9	UTSW	11	65,765,022 (GRCm39)	missense	probably damaging	1.00
PIT4280001:Dnah9	UTSW	11	65,895,839 (GRCm39)	missense	probably benign	0.44
R0021:Dnah9	UTSW	11	65,860,805 (GRCm39)	missense	probably benign	0.36
R0021:Dnah9	UTSW	11	65,860,805 (GRCm39)	missense	probably benign	0.36
R0025:Dnah9	UTSW	11	65,860,781 (GRCm39)	splice site	probably benign
R0025:Dnah9	UTSW	11	65,860,781 (GRCm39)	splice site	probably benign
R0070:Dnah9	UTSW	11	66,050,866 (GRCm39)	missense	probably benign	0.10
R0164:Dnah9	UTSW	11	65,809,630 (GRCm39)	nonsense	probably null
R0164:Dnah9	UTSW	11	65,809,630 (GRCm39)	nonsense	probably null
R0180:Dnah9	UTSW	11	66,038,116 (GRCm39)	missense	probably damaging	1.00
R0195:Dnah9	UTSW	11	65,786,731 (GRCm39)	missense	probably benign	0.30
R0230:Dnah9	UTSW	11	65,746,141 (GRCm39)	missense	probably damaging	1.00
R0243:Dnah9	UTSW	11	65,802,678 (GRCm39)	missense	possibly damaging	0.91
R0279:Dnah9	UTSW	11	65,802,615 (GRCm39)	critical splice donor site	probably null
R0288:Dnah9	UTSW	11	65,915,960 (GRCm39)	critical splice donor site	probably null
R0309:Dnah9	UTSW	11	65,917,798 (GRCm39)	splice site	probably benign
R0356:Dnah9	UTSW	11	66,021,388 (GRCm39)	critical splice donor site	probably null
R0403:Dnah9	UTSW	11	65,975,615 (GRCm39)	missense	possibly damaging	0.90
R0413:Dnah9	UTSW	11	65,998,961 (GRCm39)	missense	probably damaging	1.00
R0448:Dnah9	UTSW	11	65,809,539 (GRCm39)	splice site	probably benign
R0496:Dnah9	UTSW	11	65,965,961 (GRCm39)	missense	probably null	1.00
R0557:Dnah9	UTSW	11	65,975,492 (GRCm39)	missense	probably damaging	1.00
R0584:Dnah9	UTSW	11	65,881,315 (GRCm39)	missense	probably damaging	1.00
R0598:Dnah9	UTSW	11	66,009,703 (GRCm39)	missense	probably benign	0.02
R0599:Dnah9	UTSW	11	65,856,515 (GRCm39)	missense	probably damaging	1.00
R0606:Dnah9	UTSW	11	65,732,159 (GRCm39)	missense	probably damaging	1.00
R0666:Dnah9	UTSW	11	65,976,284 (GRCm39)	missense	probably benign	0.01
R0715:Dnah9	UTSW	11	65,972,074 (GRCm39)	splice site	probably benign
R0726:Dnah9	UTSW	11	65,856,507 (GRCm39)	missense	probably damaging	1.00
R0737:Dnah9	UTSW	11	65,998,724 (GRCm39)	missense	probably damaging	1.00
R0763:Dnah9	UTSW	11	66,046,356 (GRCm39)	missense	probably benign	0.30
R0792:Dnah9	UTSW	11	65,786,827 (GRCm39)	missense	possibly damaging	0.84
R0829:Dnah9	UTSW	11	65,896,002 (GRCm39)	missense	probably benign	0.00
R0973:Dnah9	UTSW	11	65,896,663 (GRCm39)	splice site	probably null
R0974:Dnah9	UTSW	11	65,896,663 (GRCm39)	splice site	probably null
R1055:Dnah9	UTSW	11	66,050,837 (GRCm39)	missense	probably damaging	1.00
R1081:Dnah9	UTSW	11	65,975,703 (GRCm39)	missense	probably damaging	0.99
R1184:Dnah9	UTSW	11	65,975,438 (GRCm39)	critical splice donor site	probably null
R1225:Dnah9	UTSW	11	65,761,886 (GRCm39)	missense	possibly damaging	0.94
R1304:Dnah9	UTSW	11	65,818,414 (GRCm39)	missense	probably damaging	0.98
R1417:Dnah9	UTSW	11	65,846,573 (GRCm39)	missense	probably damaging	0.96
R1439:Dnah9	UTSW	11	65,764,958 (GRCm39)	missense	probably benign	0.22
R1447:Dnah9	UTSW	11	65,999,308 (GRCm39)	missense	possibly damaging	0.65
R1450:Dnah9	UTSW	11	65,818,612 (GRCm39)	missense	probably damaging	1.00
R1470:Dnah9	UTSW	11	65,818,648 (GRCm39)	missense	probably benign	0.11
R1470:Dnah9	UTSW	11	65,818,648 (GRCm39)	missense	probably benign	0.11
R1486:Dnah9	UTSW	11	65,725,098 (GRCm39)	missense	probably damaging	1.00
R1519:Dnah9	UTSW	11	65,772,587 (GRCm39)	missense	probably damaging	0.96
R1570:Dnah9	UTSW	11	66,003,156 (GRCm39)	missense	probably benign
R1617:Dnah9	UTSW	11	65,786,747 (GRCm39)	missense	probably damaging	1.00
R1623:Dnah9	UTSW	11	65,928,463 (GRCm39)	missense	probably damaging	1.00
R1626:Dnah9	UTSW	11	65,976,093 (GRCm39)	missense	probably benign	0.05
R1671:Dnah9	UTSW	11	65,818,789 (GRCm39)	missense	probably damaging	0.99
R1694:Dnah9	UTSW	11	65,845,650 (GRCm39)	nonsense	probably null
R1701:Dnah9	UTSW	11	65,802,750 (GRCm39)	missense	probably damaging	1.00
R1702:Dnah9	UTSW	11	65,976,021 (GRCm39)	missense	possibly damaging	0.72
R1708:Dnah9	UTSW	11	65,805,980 (GRCm39)	missense	probably benign	0.11
R1718:Dnah9	UTSW	11	66,058,905 (GRCm39)	missense	possibly damaging	0.82
R1729:Dnah9	UTSW	11	65,975,846 (GRCm39)	missense	possibly damaging	0.51
R1760:Dnah9	UTSW	11	65,872,048 (GRCm39)	missense	probably benign	0.31
R1784:Dnah9	UTSW	11	65,975,846 (GRCm39)	missense	possibly damaging	0.51
R1793:Dnah9	UTSW	11	66,010,420 (GRCm39)	critical splice donor site	probably null
R1801:Dnah9	UTSW	11	65,846,123 (GRCm39)	missense	probably damaging	0.99
R1827:Dnah9	UTSW	11	65,740,887 (GRCm39)	missense	probably damaging	0.97
R1836:Dnah9	UTSW	11	66,009,667 (GRCm39)	missense	probably benign	0.10
R1840:Dnah9	UTSW	11	65,725,024 (GRCm39)	nonsense	probably null
R1847:Dnah9	UTSW	11	65,725,212 (GRCm39)	missense	probably damaging	1.00
R1872:Dnah9	UTSW	11	65,928,316 (GRCm39)	missense	probably benign	0.16
R1929:Dnah9	UTSW	11	65,867,224 (GRCm39)	missense	probably benign	0.05
R1969:Dnah9	UTSW	11	65,739,197 (GRCm39)	missense	probably damaging	1.00
R1971:Dnah9	UTSW	11	65,739,197 (GRCm39)	missense	probably damaging	1.00
R2027:Dnah9	UTSW	11	65,846,164 (GRCm39)	missense	probably benign	0.11
R2049:Dnah9	UTSW	11	65,935,509 (GRCm39)	missense	probably damaging	1.00
R2064:Dnah9	UTSW	11	66,036,261 (GRCm39)	missense	probably benign	0.31
R2104:Dnah9	UTSW	11	65,951,950 (GRCm39)	missense	probably damaging	1.00
R2109:Dnah9	UTSW	11	65,928,411 (GRCm39)	missense	probably damaging	1.00
R2160:Dnah9	UTSW	11	66,008,309 (GRCm39)	missense	probably damaging	1.00
R2172:Dnah9	UTSW	11	65,963,605 (GRCm39)	missense	probably damaging	1.00
R2198:Dnah9	UTSW	11	65,750,325 (GRCm39)	missense	possibly damaging	0.50
R2271:Dnah9	UTSW	11	66,003,188 (GRCm39)	missense	probably benign	0.37
R2272:Dnah9	UTSW	11	66,003,188 (GRCm39)	missense	probably benign	0.37
R2396:Dnah9	UTSW	11	65,975,984 (GRCm39)	missense	probably benign	0.01
R2398:Dnah9	UTSW	11	65,806,029 (GRCm39)	missense	probably damaging	1.00
R2418:Dnah9	UTSW	11	65,986,241 (GRCm39)	nonsense	probably null
R2419:Dnah9	UTSW	11	65,986,241 (GRCm39)	nonsense	probably null
R2510:Dnah9	UTSW	11	65,895,995 (GRCm39)	missense	probably damaging	1.00
R2680:Dnah9	UTSW	11	65,924,751 (GRCm39)	missense	probably benign	0.00
R2875:Dnah9	UTSW	11	66,059,287 (GRCm39)	missense	possibly damaging	0.89
R2979:Dnah9	UTSW	11	66,008,414 (GRCm39)	missense	possibly damaging	0.89
R3236:Dnah9	UTSW	11	65,845,815 (GRCm39)	missense	probably benign	0.11
R3237:Dnah9	UTSW	11	65,845,815 (GRCm39)	missense	probably benign	0.11
R3433:Dnah9	UTSW	11	65,965,938 (GRCm39)	missense	possibly damaging	0.85
R3737:Dnah9	UTSW	11	66,047,734 (GRCm39)	nonsense	probably null
R3820:Dnah9	UTSW	11	65,741,829 (GRCm39)	critical splice donor site	probably null
R3821:Dnah9	UTSW	11	65,741,829 (GRCm39)	critical splice donor site	probably null
R3822:Dnah9	UTSW	11	65,741,829 (GRCm39)	critical splice donor site	probably null
R3861:Dnah9	UTSW	11	65,943,820 (GRCm39)	splice site	probably benign
R3918:Dnah9	UTSW	11	65,761,800 (GRCm39)	missense	possibly damaging	0.54
R4011:Dnah9	UTSW	11	65,725,290 (GRCm39)	missense	probably damaging	0.98
R4044:Dnah9	UTSW	11	66,024,461 (GRCm39)	missense	probably benign	0.03
R4072:Dnah9	UTSW	11	65,975,730 (GRCm39)	missense	probably benign	0.00
R4076:Dnah9	UTSW	11	65,975,730 (GRCm39)	missense	probably benign	0.00
R4097:Dnah9	UTSW	11	65,881,285 (GRCm39)	missense	probably damaging	1.00
R4409:Dnah9	UTSW	11	65,976,303 (GRCm39)	missense	possibly damaging	0.51
R4410:Dnah9	UTSW	11	65,976,303 (GRCm39)	missense	possibly damaging	0.51
R4417:Dnah9	UTSW	11	65,872,040 (GRCm39)	missense	possibly damaging	0.75
R4420:Dnah9	UTSW	11	66,009,575 (GRCm39)	missense	probably benign	0.00
R4434:Dnah9	UTSW	11	65,998,901 (GRCm39)	missense	possibly damaging	0.67
R4451:Dnah9	UTSW	11	65,772,467 (GRCm39)	missense	probably benign	0.07
R4452:Dnah9	UTSW	11	65,917,908 (GRCm39)	missense	probably damaging	0.96
R4454:Dnah9	UTSW	11	66,038,215 (GRCm39)	missense	probably damaging	0.96
R4551:Dnah9	UTSW	11	65,732,192 (GRCm39)	missense	probably damaging	1.00
R4552:Dnah9	UTSW	11	65,732,192 (GRCm39)	missense	probably damaging	1.00
R4590:Dnah9	UTSW	11	65,931,218 (GRCm39)	missense	probably damaging	1.00
R4595:Dnah9	UTSW	11	66,058,978 (GRCm39)	missense	probably benign
R4655:Dnah9	UTSW	11	65,846,558 (GRCm39)	missense	probably benign	0.00
R4667:Dnah9	UTSW	11	66,046,357 (GRCm39)	missense	probably benign
R4718:Dnah9	UTSW	11	65,976,299 (GRCm39)	missense	probably benign
R4720:Dnah9	UTSW	11	65,967,184 (GRCm39)	missense	probably damaging	1.00
R4734:Dnah9	UTSW	11	65,724,941 (GRCm39)	missense	probably damaging	1.00
R4749:Dnah9	UTSW	11	65,724,941 (GRCm39)	missense	probably damaging	1.00
R4765:Dnah9	UTSW	11	65,818,552 (GRCm39)	missense	probably damaging	1.00
R4905:Dnah9	UTSW	11	65,764,950 (GRCm39)	nonsense	probably null
R4963:Dnah9	UTSW	11	65,975,437 (GRCm39)	splice site	probably null
R5074:Dnah9	UTSW	11	65,740,866 (GRCm39)	missense	probably damaging	1.00
R5230:Dnah9	UTSW	11	65,975,492 (GRCm39)	missense	probably damaging	0.99
R5262:Dnah9	UTSW	11	66,003,159 (GRCm39)	missense	probably benign	0.34
R5364:Dnah9	UTSW	11	65,772,522 (GRCm39)	missense	possibly damaging	0.93
R5370:Dnah9	UTSW	11	65,920,180 (GRCm39)	missense	probably damaging	1.00
R5386:Dnah9	UTSW	11	65,920,182 (GRCm39)	missense	probably damaging	1.00
R5389:Dnah9	UTSW	11	65,986,140 (GRCm39)	nonsense	probably null
R5541:Dnah9	UTSW	11	66,036,162 (GRCm39)	missense	probably damaging	1.00
R5560:Dnah9	UTSW	11	65,772,566 (GRCm39)	missense	probably benign	0.00
R5576:Dnah9	UTSW	11	65,724,922 (GRCm39)	splice site	probably null
R5648:Dnah9	UTSW	11	65,818,581 (GRCm39)	missense	probably benign	0.00
R5653:Dnah9	UTSW	11	65,740,806 (GRCm39)	missense	probably damaging	0.99
R5713:Dnah9	UTSW	11	65,916,049 (GRCm39)	missense	possibly damaging	0.92
R5763:Dnah9	UTSW	11	65,846,065 (GRCm39)	missense	probably damaging	1.00
R5825:Dnah9	UTSW	11	66,017,427 (GRCm39)	missense	probably benign	0.01
R5831:Dnah9	UTSW	11	65,998,947 (GRCm39)	missense	probably benign	0.00
R5847:Dnah9	UTSW	11	65,986,066 (GRCm39)	frame shift	probably null
R5870:Dnah9	UTSW	11	65,976,036 (GRCm39)	missense	probably benign	0.01
R5902:Dnah9	UTSW	11	65,916,013 (GRCm39)	missense	probably benign	0.08
R5918:Dnah9	UTSW	11	65,725,025 (GRCm39)	missense	probably damaging	1.00
R5979:Dnah9	UTSW	11	65,725,307 (GRCm39)	missense	probably damaging	1.00
R6065:Dnah9	UTSW	11	66,036,223 (GRCm39)	missense	possibly damaging	0.65
R6065:Dnah9	UTSW	11	65,746,164 (GRCm39)	missense	probably benign	0.05
R6086:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
R6086:Dnah9	UTSW	11	65,880,741 (GRCm39)	missense	probably damaging	0.99
R6102:Dnah9	UTSW	11	65,881,342 (GRCm39)	missense	probably damaging	0.97
R6120:Dnah9	UTSW	11	66,038,225 (GRCm39)	missense	probably benign
R6154:Dnah9	UTSW	11	65,746,164 (GRCm39)	missense	probably benign	0.00
R6262:Dnah9	UTSW	11	65,772,631 (GRCm39)	splice site	probably null
R6265:Dnah9	UTSW	11	66,058,920 (GRCm39)	missense	probably benign	0.04
R6290:Dnah9	UTSW	11	65,732,201 (GRCm39)	missense	probably damaging	1.00
R6345:Dnah9	UTSW	11	65,928,519 (GRCm39)	missense	probably damaging	0.97
R6357:Dnah9	UTSW	11	65,765,022 (GRCm39)	missense	probably damaging	1.00
R6534:Dnah9	UTSW	11	65,846,074 (GRCm39)	missense	probably damaging	0.99
R6574:Dnah9	UTSW	11	66,059,107 (GRCm39)	missense	probably benign	0.37
R6582:Dnah9	UTSW	11	65,951,923 (GRCm39)	missense	probably damaging	1.00
R6700:Dnah9	UTSW	11	65,846,192 (GRCm39)	missense	probably damaging	1.00
R6800:Dnah9	UTSW	11	65,963,565 (GRCm39)	critical splice donor site	probably null
R6812:Dnah9	UTSW	11	65,872,155 (GRCm39)	missense	probably damaging	0.99
R6931:Dnah9	UTSW	11	66,008,452 (GRCm39)	missense	possibly damaging	0.63
R6944:Dnah9	UTSW	11	65,975,975 (GRCm39)	missense	possibly damaging	0.91
R6958:Dnah9	UTSW	11	65,967,167 (GRCm39)	missense	probably damaging	1.00
R6977:Dnah9	UTSW	11	65,998,735 (GRCm39)	missense	probably benign	0.37
R7021:Dnah9	UTSW	11	65,872,057 (GRCm39)	missense	probably benign
R7161:Dnah9	UTSW	11	65,746,198 (GRCm39)	nonsense	probably null
R7175:Dnah9	UTSW	11	66,024,463 (GRCm39)	missense	probably benign	0.03
R7199:Dnah9	UTSW	11	66,009,770 (GRCm39)	missense	probably benign	0.04
R7231:Dnah9	UTSW	11	65,856,473 (GRCm39)	missense	probably damaging	1.00
R7284:Dnah9	UTSW	11	65,881,302 (GRCm39)	missense	probably damaging	0.99
R7314:Dnah9	UTSW	11	65,880,677 (GRCm39)	missense	probably benign	0.00
R7350:Dnah9	UTSW	11	65,971,404 (GRCm39)	missense	probably damaging	1.00
R7420:Dnah9	UTSW	11	66,008,233 (GRCm39)	critical splice donor site	probably null
R7427:Dnah9	UTSW	11	65,846,045 (GRCm39)	missense	probably benign
R7477:Dnah9	UTSW	11	65,883,557 (GRCm39)	missense	probably damaging	0.98
R7515:Dnah9	UTSW	11	65,732,240 (GRCm39)	missense	probably benign	0.01
R7521:Dnah9	UTSW	11	65,880,663 (GRCm39)	missense	probably damaging	0.98
R7573:Dnah9	UTSW	11	66,016,041 (GRCm39)	missense	probably benign	0.43
R7659:Dnah9	UTSW	11	65,880,606 (GRCm39)	missense	probably damaging	0.99
R7707:Dnah9	UTSW	11	66,009,784 (GRCm39)	missense	probably damaging	1.00
R7749:Dnah9	UTSW	11	65,802,656 (GRCm39)	missense	probably damaging	1.00
R7792:Dnah9	UTSW	11	65,740,839 (GRCm39)	missense	probably damaging	1.00
R7808:Dnah9	UTSW	11	65,896,631 (GRCm39)	nonsense	probably null
R7814:Dnah9	UTSW	11	65,896,486 (GRCm39)	missense	probably damaging	1.00
R7818:Dnah9	UTSW	11	65,916,037 (GRCm39)	missense	possibly damaging	0.64
R7890:Dnah9	UTSW	11	65,962,898 (GRCm39)	missense	probably damaging	0.99
R7976:Dnah9	UTSW	11	65,732,227 (GRCm39)	missense	possibly damaging	0.91
R8121:Dnah9	UTSW	11	65,908,201 (GRCm39)	missense	probably benign	0.02
R8232:Dnah9	UTSW	11	65,746,149 (GRCm39)	missense	possibly damaging	0.91
R8311:Dnah9	UTSW	11	65,880,644 (GRCm39)	missense	probably benign	0.00
R8326:Dnah9	UTSW	11	66,008,452 (GRCm39)	missense	probably benign	0.01
R8338:Dnah9	UTSW	11	65,732,067 (GRCm39)	critical splice donor site	probably null
R8356:Dnah9	UTSW	11	66,047,764 (GRCm39)	missense	probably damaging	0.99
R8456:Dnah9	UTSW	11	66,047,764 (GRCm39)	missense	probably damaging	0.99
R8468:Dnah9	UTSW	11	65,722,556 (GRCm39)	missense	probably benign	0.00
R8721:Dnah9	UTSW	11	65,986,124 (GRCm39)	missense	probably damaging	1.00
R8747:Dnah9	UTSW	11	65,818,816 (GRCm39)	missense	possibly damaging	0.69
R8798:Dnah9	UTSW	11	65,796,057 (GRCm39)	missense	probably damaging	0.99
R8806:Dnah9	UTSW	11	65,750,309 (GRCm39)	missense	probably damaging	1.00
R8826:Dnah9	UTSW	11	65,740,742 (GRCm39)	missense	probably benign	0.13
R8837:Dnah9	UTSW	11	65,746,060 (GRCm39)	missense	possibly damaging	0.72
R8886:Dnah9	UTSW	11	65,943,840 (GRCm39)	missense	probably damaging	1.00
R8887:Dnah9	UTSW	11	65,746,210 (GRCm39)	missense	probably benign	0.01
R8921:Dnah9	UTSW	11	65,802,747 (GRCm39)	missense	probably benign
R8933:Dnah9	UTSW	11	65,746,078 (GRCm39)	missense	possibly damaging	0.88
R8949:Dnah9	UTSW	11	66,059,226 (GRCm39)	missense	possibly damaging	0.91
R8967:Dnah9	UTSW	11	66,015,938 (GRCm39)	critical splice donor site	probably null
R8979:Dnah9	UTSW	11	65,895,978 (GRCm39)	missense	probably benign
R8991:Dnah9	UTSW	11	65,777,506 (GRCm39)	missense	probably damaging	0.96
R9016:Dnah9	UTSW	11	65,998,856 (GRCm39)	missense	probably damaging	0.99
R9025:Dnah9	UTSW	11	65,896,651 (GRCm39)	missense	probably damaging	1.00
R9043:Dnah9	UTSW	11	65,845,680 (GRCm39)	missense
R9047:Dnah9	UTSW	11	65,962,925 (GRCm39)	missense	possibly damaging	0.89
R9076:Dnah9	UTSW	11	66,008,464 (GRCm39)	missense	probably benign	0.21
R9113:Dnah9	UTSW	11	65,880,713 (GRCm39)	missense	probably damaging	1.00
R9152:Dnah9	UTSW	11	66,021,457 (GRCm39)	missense	probably damaging	1.00
R9187:Dnah9	UTSW	11	65,895,972 (GRCm39)	missense	probably benign
R9203:Dnah9	UTSW	11	65,746,113 (GRCm39)	missense	possibly damaging	0.58
R9234:Dnah9	UTSW	11	65,924,751 (GRCm39)	missense	possibly damaging	0.68
R9245:Dnah9	UTSW	11	65,786,731 (GRCm39)	missense	probably benign	0.30
R9265:Dnah9	UTSW	11	65,732,081 (GRCm39)	missense	probably benign	0.01
R9307:Dnah9	UTSW	11	65,976,300 (GRCm39)	missense	probably benign	0.14
R9336:Dnah9	UTSW	11	65,761,775 (GRCm39)	missense	probably damaging	1.00
R9386:Dnah9	UTSW	11	65,838,368 (GRCm39)	missense	probably damaging	1.00
R9498:Dnah9	UTSW	11	65,739,199 (GRCm39)	missense	probably damaging	0.99
R9508:Dnah9	UTSW	11	65,725,089 (GRCm39)	missense	probably damaging	1.00
R9524:Dnah9	UTSW	11	65,976,309 (GRCm39)	missense	possibly damaging	0.92
R9577:Dnah9	UTSW	11	65,867,347 (GRCm39)	missense	probably benign	0.00
R9583:Dnah9	UTSW	11	65,856,507 (GRCm39)	missense	probably damaging	1.00
R9587:Dnah9	UTSW	11	65,999,217 (GRCm39)	missense	probably null	0.92
R9612:Dnah9	UTSW	11	65,818,475 (GRCm39)	missense	probably benign	0.00
R9748:Dnah9	UTSW	11	65,976,290 (GRCm39)	missense	possibly damaging	0.51
R9749:Dnah9	UTSW	11	65,986,202 (GRCm39)	missense	probably damaging	1.00
R9759:Dnah9	UTSW	11	65,965,944 (GRCm39)	missense	probably null	0.93
R9784:Dnah9	UTSW	11	65,975,960 (GRCm39)	missense	probably damaging	0.99
V3553:Dnah9	UTSW	11	65,860,902 (GRCm39)	missense	probably damaging	1.00
X0027:Dnah9	UTSW	11	65,976,305 (GRCm39)	missense	probably benign	0.07
X0028:Dnah9	UTSW	11	65,881,278 (GRCm39)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	65,860,910 (GRCm39)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	65,818,679 (GRCm39)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	65,786,798 (GRCm39)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	65,963,661 (GRCm39)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	65,928,300 (GRCm39)	missense	probably damaging	1.00
Z1177:Dnah9	UTSW	11	66,017,476 (GRCm39)	missense	probably damaging	1.00
Z1186:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
Z1186:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1187:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1187:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
Z1188:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1188:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
Z1189:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1189:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
Z1190:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1190:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
Z1191:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1191:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
Z1192:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1192:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- CTGCTCAGCCAAAAGATCATTG -3'
(R):5'- TGCCCACTTTCACCAGTACATG -3'

Sequencing Primer
(F):5'- CCAGAGGAGCAGTGTCCAATTTATC -3'
(R):5'- CACTTTCACCAGTACATGAGGTTG -3'

Posted On

2022-02-07